Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kristina V. Kitaeva"'
Autor:
Alisa A. Shaimardanova, Daria S. Chulpanova, Valeriya V. Solovyeva, Aysilu I. Mullagulova, Kristina V. Kitaeva, Cinzia Allegrucci, Albert A. Rizvanov
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Metachromatic leukodystrophy is a lysosomal storage disease, which is characterized by damage of the myelin sheath that covers most of nerve fibers of the central and peripheral nervous systems. The disease occurs due to a deficiency of the lysosomal
Externí odkaz:
https://doaj.org/article/cc5e023c74c342fdb7e5f7ad0b3c0165
Autor:
Valeriya V. Solovyeva, Alisa A. Shaimardanova, Daria S. Chulpanova, Kristina V. Kitaeva, Lisa Chakrabarti, Albert A. Rizvanov
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
Tay-Sachs disease belongs to the group of autosomal-recessive lysosomal storage metabolic disorders. This disease is caused by β-hexosaminidase A (HexA) enzyme deficiency due to various mutations in α-subunit gene of this enzyme, resulting in GM2 g
Externí odkaz:
https://doaj.org/article/9f9bc835e2414b2699027f94ede7864d
Autor:
Daria S. Chulpanova, Aysilu I. Mullagulova, Albert A. Rizvanov, Valeriya V. Solovyeva, Kristina V. Kitaeva, Alisa A. Shaimardanova, Cinzia Allegrucci
Publikováno v:
Frontiers in Medicine
Frontiers in Medicine, Vol 7 (2020)
Frontiers in Medicine, Vol 7 (2020)
Metachromatic leukodystrophy is a lysosomal storage disease, which is characterized by damage of the myelin sheath that covers most of nerve fibers of the central and peripheral nervous systems. The disease occurs due to a deficiency of the lysosomal
Autor:
Alisa A. Shaimardanova, Daria S. Chulpanova, Lisa Chakrabarti, Albert A. Rizvanov, Valeriya V. Solovyeva, Kristina V. Kitaeva
Publikováno v:
Frontiers in Physiology
Frontiers in Physiology, Vol 9 (2018)
Frontiers in Physiology, Vol 9 (2018)
Tay-Sachs disease belongs to the group of autosomal-recessive lysosomal storage metabolic disorders. This disease is caused by β-hexosaminidase A (HexA) enzyme deficiency due to various mutations in α-subunit gene of this enzyme, resulting in GM2 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edfb23fe044abe519f0820a1f987d37a
https://nottingham-repository.worktribe.com/file/1603711/1/fphys-09-01663
https://nottingham-repository.worktribe.com/file/1603711/1/fphys-09-01663